Publications by authors named "Shojiro Okamoto"

Background: The importance of the ratio of creatinine to urinary protein, albumin, and low-molecular weight protein as a urinary marker in chronic kidney disease patients is widely recognized. However, no reference values have hitherto been established for these markers in Japanese children. The present study aimed to establish the reference values for these urinary markers in Japanese children.

View Article and Find Full Text PDF
Article Synopsis
  • The study focuses on congenital anomalies of the kidney and urinary tract (CAKUT) as a leading cause of chronic kidney disease (CKD) in children, identifying effective urine analysis methods to detect kidney dysfunction.
  • Researchers compared the efficacy of urine alpha 1-microglobulin (AMCR) and beta 2-microglobulin (BMCR) ratios against conventional urine dipstick tests and other parameters like protein and albumin-to-creatinine ratios.
  • Results showed that AMCR and BMCR are more effective for detecting CAKUT in children with stage 3-4 CKD, with high sensitivity and specificity, but further validation for AMCR is needed. *
View Article and Find Full Text PDF

Background: The long-term outcome of pediatric IgA nephropathy (IgAN) is unclear. Objective IgAN remission criteria were proposed by the Japanese Society of Nephrology in 2013.

Methods: Children with newly developed IgAN followed for >5 years were analyzed.

View Article and Find Full Text PDF

Renovascular hypertension (RVH) in children is a relatively rare disease, but it is important in that it is a treatable condition when properly diagnosed. Percutaneous transluminal renal angioplasty (PTRA) with or without stenting is widely applied to adult patients with RVH. However, limited information is available as to PTRA with stenting in pediatric patients.

View Article and Find Full Text PDF

We experienced a case of a 2-year-old boy, who presented with steroid resistant nephrotic syndrome, which developed insidiously. Renal biopsy revealed that he had focal and segmental glomerulosclerosis on light microscopy, dominant mesangial deposition of C1q by immunofluorescent staining, and electron dense deposits on electron microscopy, which are all compatible with C1q nephropathy. He had no clinical sign of any collagen diseases, including systemic lupus erythematodes.

View Article and Find Full Text PDF